These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 17476820)

  • 1. Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.
    McLean WH; Irvine AD
    Ulster Med J; 2007 May; 76(2):72-82. PubMed ID: 17476820
    [No Abstract]   [Full Text] [Related]  

  • 2. Harlequin ichthyosis. Variability in expression and hypothesis for disease mechanism.
    Dale BA; Kam E
    Arch Dermatol; 1993 Nov; 129(11):1471-7. PubMed ID: 7694551
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial occurrence of a congenital defect of the keratinisation of the skin in German Angus calves].
    Schulze U; Kuiper H; Wöhlke A; Wohlsein P; Gerhauser I; Marxfeld H; Haas L; Distl O
    Dtsch Tierarztl Wochenschr; 2007 Jan; 114(1):25-9. PubMed ID: 17252933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The perennial problem of keratinisation disorders].
    Dereure O
    Ann Dermatol Venereol; 2013 Mar; 140(3):240-1. PubMed ID: 23466163
    [No Abstract]   [Full Text] [Related]  

  • 5. The molecular basis of inherited disorders of keratinization.
    Dunnill MG
    Hosp Med; 1998 Jan; 59(1):17-22. PubMed ID: 9798559
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ichthyosis Curth-Macklin: a new sporadic case with immunohistochemical study of keratin expression.
    Brusasco A; Cavalli R; Cambiaghi S; Tadini G; Berti E; Caputo R
    Arch Dermatol; 1994 Aug; 130(8):1077-9. PubMed ID: 7519838
    [No Abstract]   [Full Text] [Related]  

  • 7. Inherited disorders of corneocyte proteins.
    Elias PM; Williams ML; Crumrine D; Schmuth M
    Curr Probl Dermatol; 2010; 39():98-131. PubMed ID: 20838039
    [No Abstract]   [Full Text] [Related]  

  • 8. Focuses solely on generalized, inherited (Mendelian) disorders of cornification (DOC or MeDOC). Introduction.
    Elias PM; Williams ML; Crumrine D; Schmuth M
    Curr Probl Dermatol; 2010; 39():1-29. PubMed ID: 20838036
    [No Abstract]   [Full Text] [Related]  

  • 9. Defects in the barrier.
    Roop D
    Science; 1995 Jan; 267(5197):474-5. PubMed ID: 7529942
    [No Abstract]   [Full Text] [Related]  

  • 10. Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormal.
    Fleckman P; Holbrook KA; Dale BA; Sybert VP
    J Invest Dermatol; 1987 May; 88(5):640-5. PubMed ID: 2437218
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Keratins and skin disorders.
    Lane EB; McLean WH
    J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)].
    Anton-Lamprecht I
    Arch Dermatol Forsch; 1973 Dec; 248(2):149-72. PubMed ID: 4780660
    [No Abstract]   [Full Text] [Related]  

  • 13. An autosomal recessive exfoliative ichthyosis with linkage to chromosome 12q13.
    Hatsell SJ; Stevens H; Jackson AP; Kelsell DP; Zvulunov A
    Br J Dermatol; 2003 Jul; 149(1):174-80. PubMed ID: 12890214
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Altered keratin expression in ichthyosis hystrix Curth-Macklin. A light and electron microscopic study.
    Niemi KM; Virtanen I; Kanerva L; Muttilainen M
    Arch Dermatol Res; 1990; 282(4):227-33. PubMed ID: 1695499
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The growth of ichthyotic epidermal cells in a 3-dimensional reconstruction of human skin, the skin equivalent.
    Featherstone J; Dykes PJ; Marks R
    Clin Exp Dermatol; 1995 Jul; 20(4):313-8. PubMed ID: 8548989
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa.
    Steijlen PM; Kremer H; Vakilzadeh F; Happle R; Lavrijsen AP; Ropers HH; Mariman EC
    J Invest Dermatol; 1994 Sep; 103(3):282-5. PubMed ID: 7521372
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Are ichthyosis follicularis and hereditary mucoepithelial dystrophy related diseases.
    Rothe MJ; Lucky AW
    Pediatr Dermatol; 1995 Jun; 12(2):195. PubMed ID: 7659652
    [No Abstract]   [Full Text] [Related]  

  • 18. Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-Macklin.
    Bonifas JM; Bare JW; Chen MA; Ranki A; Neimi KM; Epstein EH
    J Invest Dermatol; 1993 Dec; 101(6):890-1. PubMed ID: 7504030
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis.
    Anton-Lamprecht I; Schnyder UW
    Clin Genet; 1976 Oct; 10(4):245-7. PubMed ID: 61827
    [No Abstract]   [Full Text] [Related]  

  • 20. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
    Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
    Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.